Search Images Maps Play YouTube News Gmail Drive More »
Sign in
Screen reader users: click this link for accessible mode. Accessible mode has the same essential features but works better with your reader.


  1. Advanced Patent Search
Publication numberUS3839274 A
Publication typeGrant
Publication dateOct 1, 1974
Filing dateApr 16, 1973
Priority dateNov 3, 1969
Publication numberUS 3839274 A, US 3839274A, US-A-3839274, US3839274 A, US3839274A
InventorsW Beears
Original AssigneeGoodrich Co B F
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Polyolefins stabilized with thiopropionamides and phenols
US 3839274 A
Highly effective stabilizer systems are obtained when bis- thio propionamides are employed in combination with certain phenols. Especially useful thio propionamides include N,N'-methylene-bis[ beta -(arylthio)propionamides] and N,N'-methylene-bis[ beta -(alkylthio)propionamides]. The phenolic stabilizers are derived from isocyanurates and 1,3,5-triazines. The combinations are particularly useful for the stabilization of polyethylene and polypropylene.
Previous page
Next page
Claims  available in
Description  (OCR text may contain errors)

United States Patent Beears I Oct. 1, 1974 POLYOLEFINS STABILIZED WITH 3,531,483 9 1970 Gi116s...; 260 248 THIOPROPIONAMIDES AND PHENOLS 3,538,092 11 1970 Dexter 260/248 Warren L. Beears, Brecksville, Ohio The B. F. Goodrich Company, New York, NY.

Filed: Apr. 16, 1973 Appl. NO.I 351,280

Related US. Application Data Continuation-in-part of Ser. No. 873,650, Nov. 3, 1969, abandoned.


As signee:

us. 01 260/458 N, 260/459 NC Int. Cl. C08f 45/60 Field of Search 260/45 .8 NT, 45.9 NC

References Cited UNlTED STATES PATENTS 5/1957 Chenicek 99/163 Primary Examiner-Melvyn l. Marquis Assistant Examiner-R. A. White Attorney, Agent, or Firm.l. Hughes Powell, Jr.

[5 7] ABSTRACT from isocyanurates and 1,3,5-triazines. The combina-' tions are particularly useful for the stabilization of polyethylene and polypropylene.

8 Claims, N0 Drawings POLYOLEF INS STABILIZED WITH THIOPROPIONAMIDES AND PHENOLS CROSS REFERENCE TO RELATED APPLICATION This application is a continuation-in-part of application Ser. No. 873,650 filed Nov. 3, 1969 now abandoned.

BACKGROUND OF THE INVENTION Although polyolefins are subject to degradation due to oxidative, thermal and photochemical effects, quite stable polyolefin compositions are obtained if small amounts of certain thio compounds are incorporated therein. Thiodipropionates, for example, are effective by themselves and in combination with other conventional stabilizers, especially phenolic stabilizers, for the stabilization of polyethylene and polypropylene.

It is desirable to obtain highly effective stabilizer systems, particularly where the stabilizer components are high molecular weight compounds since, in general, the volatility of these compounds is more favorable to high temperature processing.

SUMMARY OF THE INVENTION Excellent activity is obtained when bisthiopropiona- I mide stabilizers are employed in combination with phenolic stabilizers derived from isocyanurates or 1,3,5- triazines. The stabilizer systems are effective for the prevention of oxidative, thermal and photochemical degradation of polyolefins, particularly polyethylene and polypropylene. N,N'-methylene-bis[,B-(alkylthio)- propionamides] and N,N'-methylene-bis[B-(arylthio)- propionamides] are particularly useful when used in combination with tris(3-alkyl-4-hydroxybenzyl- )isocyanurate. The stabilizer system will be present in an amount between about 0.01 percent and 5 percent by weight of the total composition. Exceptional activity is observed in polyethylene and polypropylene when the weight ratio of the two stabilizer components is between about 5:1 to about 1:5.

DETAILED DESCRIPTION This invention relates to a new stabilizer system effective for the stabilization of polyolefins particularly polyethylene and polypropylene. The present stabilizer system contains at least one thio propionamide compound, that is, a compound containing the molecular grouping wherein R is a hydrogen or a methyl radical and R, is an alkyl group containing from eight to 24 carbon atoms, an aryl group, or an aralkyl or alkaryl group containing from six to 20 carbon atoms. Excellent results are obtained when R, is an alkyl radical containing from eight to about 18 carbon atoms or a phenyl, a benzyl or a naphthyl radical. The aryl groups may contain other substituents which do not interfere with the activity of the thio function such as halogens and similar groups. The presence of such groups on the aryl group often even enhance the activity of these compounds.

Especially useful bis-thio propionamides will utilize an alkylene radical containing from one to eight carbon; atoms, and preferably a methylene radical, as a nucleus for bonding two groups of the type (I). Excellent results have been obtained with N,N'-methylene-bis[fl- (alkylthio)propionamides] and N,N'-methylene-bis[B- (arylthio)propionamides] having the structural formula wherein R and R are the same as defined above. Compounds of the above type useful in the present invention include N,N-methylene-bis[B-(octylthio)propionamide], N,N-methylene-bis-[B-octylthio)-amethylpropionamide], N,N'-methylene-bis[B- (nonylthio )propionamide 1, (dodecylthio)propionamide], (dodecylthio )-a-methylpropionamide], N,N methylene-bis[ ,8-(tridecylthio)propionamide N,N methylene-bis[ /3( tetradecylthio )propionamide N,N- -methylene-bis[B-(hexadecylthio)propionamide], N,- N -methylene-bis ,8-( octadecylthio )propionamide N,N-methylene-bis[ti-(octadecylthio)-amethylpropionamide], N,N'-methylene-bis[B- (eicosylthio )propionamide N,N -methylene-bis[B- (phenylthio)propionamide], N,N-methylene-bis[,8- (phenylthio)-a-methylpropionamide], N,N- methylene-bis[B-(naphthylthio)propionamide], N,N- methylene-bis[B-(p-chlorobenzylthio)propionamide], N,N'-methylene-bis[B-(p-chlorobenzylthio)-amethylpropionamide], and the like.

The thio propionamide compounds are conveniently prepared by reacting a mercaptan with a compound containing acrylyl or methacrylyl substitution. For example, to obtain the N,N'-methylene-bis[B-( alkylthio)- propionamides, 2 mols of the alkyl mercaptan are reacted with 1 mol methylene-bisacrylamide or methylene-bismethacrylamide. The reactions are generally conducted in a solvent medium -in the presence of a basic catalyst. The catalyst can be an alkali or alkaline earth metal hydroxide or quaternary ammonium hydroxide such as trimethylbenzyl ammonium hydroxide or tetramethyl ammonium hydroxide. Other basic compounds including amines, such as triethyl amine, and alkali metal alkoxides, such as sodium methoxide, may also be employed to catalyze the reaction. The reaction is generally conducted at an elevated temperature not exceeding about C. To avoid undue polymerization through the acrylyl or methacrylyl groups a small amount of any conventional polymerization inhibitor, such as 2,6-di-t-butyl-p-cresol, can be added to the reaction mixture.

The stabilizer systems of the present invention, in addition to the bis- (thio propionamide), will contain at least one additional stabilizer compound. Particular advantage is obtained when the thio propionamides are employed in combination with certain other stabilizer compounds of the phenolic type having one or more hindered phenol groups substituted on a six-membered nitrogen-containing heterocyclic ring structure. The heterocyclic nucleus will contain three alternating nitrogen heteroatoms, that is, in the 1,3 and 5 ring positions. When phenolic-substituted isocyanurates or 1,3,5-triazines are used in combination with the thio propionamide compounds, the stabilization achieved N,N-methylene-bis l3- N,N '-methylene-bis[B- v '3 far surpasses that obtained with either compound alone at the same level or the sum of the individual stabilizer compounds when employed alone. A completely unexpected improvement in the stability of the olefin polymers is realized.

The phenolic substituents are preferably 4-hydroxyaryl groups containing one or two alkyl substituents immediately adjacent (ortho) to the hydroxyl group. The alkyl groups will generally contain from about one to 18 carbon atoms and more preferably will be tertiary alkyl groups containing from four to 12 carbon atoms. 2,6-Di-tertiary-butyl-4 hydroxyphenyl compounds are particularly advantageous for the present invention.

Substitution of the phenolic group onto the isocyanurate or 1,3,5-triazine rings may be achieved through a variety of linkages. For example, the phenolic moiety may be bonded to a carbon atom of the heterocyclic ring through an oxygen atom,'a sulfur atom, an imino or substituted imino group, a carboxyl group, an alkylene group or the like. In a similar manner thephenolic substituent can be bonded tojanitrog'en atom of the heterocyclic nucleus. The latter is especially advantageous with isocyanurates. In either instance, however, one, two or. three phenolic moieties may be substituted.

Particular advantage is realized whenthio propionamides are employed in combination with hydroxyphenylalkyleneyl isocyanurates of the general formula carbon atoms and more preferably a tertiary alkyl group containing from-four to eight carbon atoms, R" is hydrogen or an alkyl group containing from one to 18 carbon atoms and preferably a tertiary alkyl group containing four to eight carbon atoms positioned ortho to the hydroxyl group. Such compounds of the above,

type include: tris-( 3-methyl-4-hydroxybenzyl- )isocyanurate, tris-( 3-t-butyl-4-hydroxybenzyl- )isocyanurate, tris-( 3-t-amyl-4-hydroxybenzyl isocyanurate, tris-(3-octyl-4-hydroxybenzyl)isocyanurate, tris-(3,5-dimethyl-4-hydroxybenzyl)isocyanurate, tris- (3,5-diisopropyl-4-hydroxybenzyl)isocyanurate, tris- (3-cyclohexyl-4-hydroxybenzyl )isocyanurate, tris-( 3 ,5-

di-t-butyl-4-hydroxybenzyl )isocyanurate, tris-( 3-tbutyl-S-t-amy1-4-hydroxybenzyl)isocyanurate, tris- (3,5-di-t-amyl-4-hydroxybenzyl)isocyanurate, tris- [3,5-di-( l-methyl-1-ethylpropyl)-4-hydroxybenzyllisocyanurate, tris-[3,5-di-( l,1,2,2- tetramethylpropyl)-4-hydroxybenzyl]isocyanurate, tris-[3,5-di-('l,1-dimethylpentyl)-4-hydroxybenzyllisocyanurate and the like. Also useful are monoand (ii-substituted isocyanurates such as bis-(3-methyl-4- hydroxybenzyl )isocyanurate, bis-( 3-t-butyl-4-hydroxybenzyl)isocyanurate, bis-(3,5-dimethyl-4-hydroxsubstituted wherein R'jisan alkyl group containing' from one to 18 ybenzyl)isocyanurate, bis-(3,5-di-t-butyl- 4-hydroxybenzyl)isocyanurate, 3-methyl-4vhydroxybenzyl iso cyanurate, 3-t-butyl-4 hydroxybenzyl isocyanurate, 3,5-dimethyl-4-hydroxybenzyl isocyanurate, 3,5-di-tbutyl-4-hydroxybenzyl isocyanurate, bis-(3-methyl-4- hydroxybenzyl)hexyl isocyanurate, bis-('3-t-butyl-4- hydroxybenzyl) hexyl isocyanurate, bis-(3,5-di-t-butyl- 4-hydroxybenzyl)hexyl isocyanurate, bis-(3,5-di-tbutyl-4-hydroxybenzyDoctadecyl isocyanurate, as well as other structurally related isocyanurates which are more fully described in copending applications Ser. No. 770,863 now U.S.Pat. No. 3,531,483 and Ser. No.

770,846 now U.S. Pat. No. 3,598,815.

In addition to the above-mentioned phenolicsubstituted isocyanurates, excellent activity is observed when the bisalkylthiopropionamides are combined with 4-hydroxyaryl-substituted s-triazines such as: hexahydro- 1 ,3 ,5-tris[,B-( 3,5-di-t-butyl-4- hydroxyphenyl )propionyl]-s-triazine, hexahydro-l ,3 ,5- tris[ B-( 3 ,5-di-t-amy1-4-hydroxyphenyl )propionyl -s-' triazine, hexahydro-1,3 ,5 -tris[ ,B-( 3-t-butyl-5-t amyl-4- hydroxyphenyl)propiony1]-s-triazin'e, hexahydro-l ,3 ,5- tris[/3-( 3 ,5-di-l-methyl-1-ethylpropy1-4- hydroxyphenyl )propionyl]-s-triazine', heXahydro-1 ,3 ,5- tris[,B- (3,5-di-1,1,2,2-tetramethyl-propy1-4 I I hydroxyphenyl )propionyl]-s-triazine, hexahydrol ,3 ,5- tris[B-( 3 ,5-di-1 1 -'dirriethylpentyl-4- hydroxyphenyl )propionyl]-s-triazine, hexahydro-l ,3 ,5 tris[/3-(3,5-di-t-butyl-4-hydroxypheny1)u-methylpropionyl -s-triazine, hexahydro-1,3 ,5 -tris[ B 3 ,S-di-tamyl-4-hydroxyphe nyl )-a-'methylpropionyl ]-s-triazine, hexahydrol ,3 ,5-tris[/3-( 3 ,5 -di-t-butyl-4- hydroxyphenyl )butyryH-s-t riaZine, hexahydro-l ,3 ,5- tris[y-( 3 ,5-di-t-butyl-4-hydroxyphenyl )butyryl ]-striazine, 6-(4-hydroxy-3,S-di-r-butylanilino)-2,4-bis- (n-octylthio)-1,3,5-triazine, 6-( 4-hydroxy-3,5-dij-tbutylanilino)-2,4-bis-(phenylthio)-1,3,5-triazine, 6-( 4- hydroxy-3,S-di-t-butylanilirio)-2,4-bis-(octadecylthio)- 1',3,5-triazine, 6-(4-hydroxy-3,5-di-'t-butylanilino)-2,4- bis-cyclohexylthio-l,3,5 triazine, 6-(2-hydroxy-3,5-dit-buty1-6-methylanilino)-2,4-bis-(n octylthio)-1,3,5- triazine, 6-(4-hydroxy-3,S-di-t-butylanilino)-2,4-bis (2,3-dimethylphenylthio 1 ,3,5-'triazine, 6-(4-hydroxy- 3,5-di-t butylanilino)-2,4-bis-(carbo-h i lauryloxyethy1thio)-1,3,5 triazine, 6-(4-hydroxy-3,5- di-t-butylanilino 2,4-bis- 4-t-octylpheno xy )-1 ,3 ,5- triazine, 6-(4-hydroxy-3,S-di-t-butylanilino)-2,4-bis- (2-carbo*n-lauryloxyphenylthio)-1,3,5-triazine, 6-( 4- hydroxy-3,5-di-t-butyl-N-benzylanilino)-2,4 bis(noctylthio )-1 ,3,5-triazine, 6-( 4-hydroxy-3,5-di-tbutylanilino )-4-n-octylthi0-2-chloro-1 ,3,5-triazine, 4,- 6-bis-(4-hydroxy-3,S-di-t-butylanilino)-2-chloro-1,3 ,5- triazine, 6-(4-hydroxy-3,S-di-t-butylphenoxy)-2,4-bis- (phenoxy )-1 ,3,5-.triazine, 2,4,6-tris-(4-hydroxy-3,5-dit-butylphenoxy):1,3,5-triazine, 6-(4-hydroxy-3,5-di-tbutylphenoxy)-2,4-bis-(n-octyl-thioethylthio)-1,3 ,5- triazine, 6'-(4-hydroxy-3,5-di-t-butylphenoxy)-2,4- dichloro-1,3 ,S-triazine, 6-(4-hydroxy-3 ,S-di-tbutylphenoxy )-2,4 -bis-(n-octylthiopropylthio)-1 ,3 ,5- triazine, 2,4,6-tris-(4-hydroxy-3-methyl-5-tbutylphenoxy)-1,3,5-triazine, 2,4-bis-(4-hydroXy-3 ,5- di-t-butylphenoxy)-6-dodecylamino-1,3,5-triazine, 2,4- bis-( 4-hydroxy-3 ,S-di-t-butylphenoxy)-6-amino-1-,3 ,5 triazine, 2,4-bis-(4-hydroxy-3,5.-di-t-butylphenoxy)-6- (n-o'ctylthio)-l ,3,5-triazine, 2,4-bis-(4-hydroxy-3,5-dit-butylphenoxy )-6-( n-octylthiopropylthio l ,3 ,5- triazine, 6-(4-hydroxy-3,5-di-t-butylphenylthio)-2,4-

bis-(ethylthio)-1,3,5-triazine, 6-(4-hydroxy-3 ,S-di-tbutylphenylthio )-2,4-bis-( phenylthio )-1 ,3 ,5-triazine, 6-(4-hydroxy-3,5-di-t-butylphenylthio)-2,4-bis-(noctylamino)-1 ,3 ,5-triazine, 6-(4-hydroxy-3 ,5-di-tbutylphenylthio)-2,4-bis-(n-octyloxy)-1,3,5-triazine, 6-(4-hydroxy-3,S-di-t-butylphenylthio)-2-mercapto-4- n-octadecylthiol ,3,5-triazine, 6-(4-hydroxy-3,5-di-tbutylphenylthio)-2,4-bis-(4-t-butylphenoxy)- 1,3,5-triazine, 2,4,6-tris-(4-hydroxy-3,5-di-tbutylphenylthio)-l ,3,5-triazine, 2,4-bis-(4-hydroxy- 3,S-di-t-butylphenylthio)-6-(n-dodecylamino)-1,3,5- triazine, 2,4-bis-(4-hydroxy-3,5-di-t -butylphenylthio)- 6-amino-l,3,5-triazine, and the like.

The stabilizer systems of the present invention are useful to prevent degradation of olefin polymers. Although polypropylene and polyethylene are most advantageously stabilized, the present compositions are equally effective to stabilize other polyolefins derived from a-olefins containing up to about eight carbon atoms such as poly-4-methylpentene- 1, polybutene and the like. They are also useful to stabilize polyolefin copolymer compositions such as ethylene-propylene copolymers. Physical mixtures of olefin homopolymers and copolymers are also stabilized according to the present invention. The polyolefins may be of high density, medium density or low density. The stabilized polyolefinic materials are useful for thermoplastic molding and coating applications as well as having a wide variety of other applications well known to the art.

When employing the present combinations of stabilizers, the total amount of the stabilizer system will be between 0.01 percent and 5 percent by weight based on the total stabilized composition. Excellent results have been obtained when the total concentration of stabilizer components is between about 0.1 percent and 3 percent by weight based on the total stabilized composition. The weight ratio of the thio propionamide to the phenolic-substituted isocyanurate or 1,3,5-triazine will be varied between about 5:1 and 1:5 to obtain enhanced activity. Marked synergistic activity is obtained when the stabilizer components are employed in about a 1:1 weight ratio.

The stabilizer systems are readily incorporated employing conventional methods into the polyolefin and generally require no special processing. They are added to the polymers by mixing on a mill or in a Banbury mixer and may be added, alone, in a suitable solvent or masterbatched with other ingredients, to a solution of the polymer. The ready solubility of the stabilizer components in a wide variety of organic solvents facilitates their use in solution and also renders them compatible with most oils and lubricants. The stabilizer system can be used in conjunction with other compounding ingredients such as processing oils, plasticizers, lubricants, fillers, reinforcing agents and are also compatible with other known oxidative stabilizers, color and heat stabilizers, ultraviolet absorbers and the like.

In addition to the stabilization of polyolefins the present stabilizer systems are also useful to stabilize other polymer compositions, oils, lubricants, saturated and unsaturated hydrocarbons and like materials which are subject to oxidative attack. Polystyrene, for example, or copolymers of butadiene and styrene may be stabilized with the present compounds. Also effectively stabilized are various types of lubricating oils, fatty materials such as the oils of animal and vegetable origin, gasoline, mineral oil, diesel oil, drying oils and resins.

The following Examples serve to illustrate the invention more fully.

EXAMPLE I N,N'-methylenebis[,B-(n-octadecylthio)propionamide] was prepared. 11.3 grams (0.0735 mole) or methylenebis acrylamide, 42.0 grams (0.147 mole) of n-octadecylmercaptan, and 470 milliliters of tetrahydrofuran were put into a reactor vessel and stirred while purging the vessel with nitrogen gas. The mix was a solution of n-octadecylmercaptan in THF with the methylenebis acrylamide in suspension. 0.3 grams of sodium methoxide, NaOCH was then added. lnitial temperature was 24 C., which rose to 34-3 6 C. upon addition of the NaOCH The mix was then heated to about 60 C. for about minutes, and then allowed to cool down to about 25 C. over the next hour and stirred for 3 more hours. Total reaction time was about 5.5 hours. The reaction mix was then cooled to about 5 C. and the solid material filtered out and dried at room temperature. 38.7 grams of this product was dissolved in a hot THE-1O percent by weight water solvent, and then cooled to precipitate out a solid. This material was air dried and submitted for NMR (nuclear magnetic resonance) spectra. The product obtained was determined to be the desired octadecylthio propionamide. When n-dodecylmercaptan was used in place of n-octadecylmercaptan, the corresponding N,- N'-methylene-bis-[,B-(n-dodecylthio) propionamide] was obtained.

Preparation of tris(3,5-di-t-butyl-4-hydroxybenzyl) isocyanurate.

A reactor equipped with a stirrer, condenser and dropping funnel was charged with 200 ml. of anhydrous N,N-dimethyl formamide and 16.2 grams (0.2 mol) anhydrous potassium cyanate suspended therein. The reactor and dropping funnel were maintained under a nitrogen blanket throughout the run. The suspension was heated to 130 C. and 51 grams (0.2 mol) 3,5-di-tbutyl-4-hydroxybenzyl chloride dissolved in 50 ml. dry N,N-dimethyl formamide added dropwise over a 2 hour period. The reaction mixture was heated with stirring for an additional hour, allowed to cool and poured into ice water. The crude reaction product was recovered by filtration. Purification was achieved by multiple extraction of an ether solution of the crude product with 5 percent aqueous sodium hydrosulfite, water and saturated salt solution. The ether was removed by evaporation and the product recrystallized from methanol and water. 25 grams of the tris(3,5-di-t-butyl-4-hydroxybenzyl)isocyanurate melting at 2l32l5 C. was obtained. Infrared analysis showed a single carbonyl peak at 1,710 cm and no nitrogen-hydrogen linkages. Elemental analysis of the product agreed with the calculated values.

EXAMPLE ll The N,N-methylene-bis[,B-(n-octadecylthio) propionamide] and the tris(3,S-di-t-butyl-4hydroxybenzyl)isocyanurate prepared in Example 1 were mixed with parts by weight of polypropylene and the composition tested for its stability. The stabilizers were incorporated into the polypropylene by dissolving them in benezene, suspending the polypropylene therein, and then evaporating off the benzene under reduced pressure. The stabilized polypropylene was then run through an extruder operating at 60 rpm and at 220 C. A 100 gram. sample was taken and pressed in amold shimmed to the desired thickness (about 20 mils).

Sample Bis-thiopro- Phenolic iso- Hours pionamide cyanurate to parts/100 parts parts/I parts failure 1 none none 3 2 none 0.] M 3 0.25 0.1 456 The example shows the excellent stability of a poly- 2O Polypropylene parts by we i The example demonstrates that at about a 1 to 1 weight ratio of bis-'thiop ropionamide to phenolic isocyanurate (a l to l millimole' ratio herein), very marked syner- EXAMPLE IV It is important that the R groups on the bis-thiopropionamides contain at least six carbon atoms, and preferably from eight to about 18 carbon atoms. The size and structure of the R group gives the compound increased solubility in the polyolefin and also makes the compound less volatile at processing and operational temperatures. The compositions of the present invention were compared to compositions suggested in the art. U.S. Pat. No. 2,792,307, in Example 3, recites the preparation and use of N,N'-methylene-bis(B-ethylthio)propionamide as a stabilizer. U.S. Pat. No. 3,538,092, in Example 6, recites the use of 2,4-bis- (3 ,5-di-t-butyl-4-hydroxyphenoxy )-6-( n-octylthio l,3,5-triazine with mercaptopropionyl-s-triazine to stabilizer polypropylene. Comparisons with the art compositions were made on an equal mole basis. Compositions were prepared following the procedure in Example II, and tested for. their stability at 150 C. in an aircirculation oven. Test results and compositions-are as fQI Q ight .100 '100 1'00 Tris-( 3.5-di-t-butyl-4- hydroxybenzyl )isocyanurate millimoles N,N'-methylene-bis-(B-noctadecylthio )propionamide millimoles N,N-methylene-bis-(B- ethylthio)propionamide millimoles 2,4-bis(3,5-di-t-butyl-4- hydroxyphenoxy)-6-(n-octylthi0)-l ,3,5-triazine millimoles Hours to crazmg pressure. The stabilized samples are then hot milled for about 5 minutes at 300 i 10 F. The polypropylene is sheeted off and placed in a mold shimmed to, the desired thickness. The samples are molded at 400 F. and 4,000 psi for 2 minutes and then transferred to a cold press at 4,000 psi for a 2 minute cooling period. Equally good results are obtained when polyethylene is stabilized with the stabilizer combination of this inven- 7 EXAMPLE in Example ll was essentially repeated except that the samples were tested at l C. The compositions and' test results are as follows:

Phenolic isocyanurate' Hours Thio-propionamide' millito Sample millimoles parts moles parts crazing Sample 1 is a composition of the present invention. Samples 2 and 3 both employ the'ethylthio compound used in U.S. Pat. No. 2,792,307. It is evident that the octadecylthio compound used in Sample, 1 yields a much morev stable composition than Samples 2 and 3. Sample 3 uses a combination suggested by U.S. Pat. No. 3,538,092 with the B-ethylthio compound used in place of the mercaptopropionyl-s-triazine. Again, it is evident'that Sample 1, of the present invention, offers ma eater stabili uponpvcn gwherein R is hydrogenor a is selected from the group consisting of an alkyl radical containing from eight to 24 carbon atoms and an aryl,

aralkyl, or alkaryl radical containing six to carbon atoms, and (b) a phenolic stabilizer of the formula wherein R is an alkyl group containing from one to 18 carbon atoms and R" is hydrogen or an alkyl group containing from one to l8 carbon atoms.

2. A composition of claim 1 wherein the polyolefin polymer is polyethylene or polypropylene, and the stabilizer system is present in from about 0.1 percent to about 3 percent by weight of the composition.

3. A composition of claim 2 wherein (b) R and R" are tertiary alkyl radicals containing four to eight carbon atoms I 4. A composition of claim 3 wherein (a) R is an alkyl radical containing from eight to about 18 carbon FQ 5. A composition of claim 4 wherein (b) is tris(3,5- di-t;butyl-4 hydroxybenzyl)isocyanurate.

6. A composition of claim '5 wherein the weight ratio of (a) to (b) is about 1 to l.

7. A composition of claim 6 wherein (a) is N,N- methylene-bis(B-dodecylthio)propionamide.

8. A composition of claim 6 wherein (a) is N,N- methylene-bis( fi-octadecylthio )propionamide.

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US2792307 *Jul 20, 1953May 14, 1957Universal Oil Prod CoStabilization of organic compounds
US3531483 *Oct 25, 1968Sep 29, 1970Goodrich Co B FHydroxyphenylalkyleneyl isocyanurates
US3538092 *Dec 11, 1968Nov 3, 1970Geigy Chem CorpDerivatives of n,n',n"-tris(3-mercaptopropionyl)-hfxahydro-s-triazine
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US3975414 *May 8, 1975Aug 17, 1976The Goodyear Tire & Rubber CompanyN,N-bis(4-anilinophenyl)-4,7-dithia-5-methyldecanediamide and related compounds useful as polymer stabilizers
US4362831 *Dec 7, 1979Dec 7, 1982Adeka Argus Chemical Co., Ltd.Synergistic light and heat stabilizer compositions for synthetic resins and resin compositions containing the same
US6365701May 27, 1999Apr 2, 2002Canon Kabushiki KaishaInk-contacting member, ink-absorbing member, ink tank and ink-jet cartridge
US6634739Feb 5, 2002Oct 21, 2003Canon Kabushiki KaishaInk-contacting member, ink-absorbing member, ink tank and ink-jet cartridge
EP0960732A2 *May 28, 1999Dec 1, 1999Canon Kabushiki KaishaInk-contacting member
U.S. Classification524/101, 524/225
International ClassificationC09K15/30, C08K5/3492, C08K5/372
Cooperative ClassificationC08K5/3725, C09K15/30, C08K5/34924
European ClassificationC08K5/3492D, C08K5/372B, C09K15/30